تفاعل #3437

ord-9f95807db7ef46aaa34d1a46e928917e

معادلة التفاعل

O=C(Cl)C(=O)Cl
Oxalyl chloride
COC(=O)C(C)Oc1cccc2c1cc(C)n2Cc1ccccc1
2-[[2-methyl-1-(phenylmethyl)-1H-indol-4-yl]oxy]propanoic acid methyl ester
N
ammonia
COC(=O)C(C)Oc1cccc2c1c(C(=O)C(N)=O)c(C)n2Cc1ccccc1
2-[[3-(2-amino-1,2-dioxoethyl)-2-methyl-1-(phenylmethyl)-1H-indol-4-yl]oxy]propanoic acid, methyl ester
المردود 90.0%

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    غسيلwashed with water
  2. 2
    تجفيفdried (MgSO4)
  3. 3
    تركيزconcentrated
  4. 4
    أخرىThe residue was chromatographed on silica gel (eluted with EtOAc)

الإجراء التجريبي

Oxalyl chloride (0.16 mL, 1.9 mmol) was reacted with 480 mg (1.5 mmol) of dl-2-[[2-methyl-1-(phenylmethyl)-1H-indol-4-yl]oxy]propanoic acid methyl ester and then reacted with anhydrous ammonia as in Example 1, Part F and the reaction product was dissolved in EtOAc, washed with water, dried (MgSO4) and concentrated. The residue was chromatographed on silica gel (eluted with EtOAc) to give 531 mg (90% yield) of dl-2-[[3-(2-amino-1,2-dioxoethyl)-2-methyl-1-(phenylmethyl)-1H-indol-4-yl]oxy]propanoic acid, methyl ester, melting at approximately 175° C.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US05733923uspto-grants-1998_03